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日用化学工业(中英文) ›› 2026, Vol. 56 ›› Issue (2): 260-270.doi: 10.3969/j.issn.2097-2806.2026.02.015

• 分析与检测 • 上一篇    下一篇

基于UPLC-Q-TOF-MS与HPLC-QQQ-MS/MS对化妆品中23种局部麻醉药进行筛查与测定

杨若彤1,2,吴方园1,2,徐廣谦1,2,郭桂文1,2,王海燕2,*(),贾凌云1,*()   

  1. 1.沈阳药科大学,辽宁 沈阳 110000
    2.中国食品药品检定研究院,北京 100050
  • 收稿日期:2025-11-20 修回日期:2026-01-26 出版日期:2026-02-22 发布日期:2026-03-09
  • 基金资助:
    科技基础资源调查专项(2022FY10120203);中国食品药品检定研究院关键技术研究基金(GJJS-2022-8-1)

Screening and determination of 23 local anesthetics in cosmetics using UPLC-Q-TOF-MS and HPLC-QQQ-MS/MS

Ruotong Yang1,2,Fangyuan Wu1,2,Guangqian Xu1,2,Guiwen Guo1,2,Haiyan Wang2,*(),Lingyun Jia1,*()   

  1. 1. Shenyang Pharmaceutical University, Shenyang, Liaoning 110000, China
    2. National Institutes for Food and Drug Control, Beijing 100050, China
  • Received:2025-11-20 Revised:2026-01-26 Online:2026-02-22 Published:2026-03-09
  • Contact: E-mail: summerwhy163@163.com(Haiyan Wang);jialingyun2003@126.com(Lingyun Jia).

摘要:

实验室建立了一种高效的反相超高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF-MS)定性方法,用于筛查化妆品中超过2 000种风险物质(包括局部麻醉药,LAs),该方法已成功应用于实际样品分析。该研究旨在开发一种更简便的高效液相色谱-三重四极杆串联质谱(HPLC-QQQ-MS/MS)方法,用于LAs的定量测定。样品经甲醇超声提取后,采用安捷伦Poroshell 120 EC-C18色谱柱(2.1 mm × 100 mm,2.7 μm)进行分离,以0.1%甲酸水溶液和甲醇为流动相进行梯度洗脱,采用外标法进行定量分析。结果表明,23种LAs在12 min内实现有效分离,在对应浓度范围内线性关系良好,相关系数均大于0.99;检出限为0.002 5~0.05 μg/g,定量限为0.01~0.1 μg/g;在5种空白化妆品基质中,23种LAs的平均回收率为80.68%~117.57%,相对标准偏差均小于5.98%。该方法精密度良好、准确度高,适用于5种化妆品基质中LAs的测定。

关键词: 局部麻醉药, 分析化学, 超高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF-MS), 高效液相色谱-三重四极杆串联质谱(HPLC-QQQ-MS/MS)

Abstract:

The laboratory established an efficient reversed-phase ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry(UPLC-Q-TOF-MS)qualitative method for screening more than 2 000 kinds of risk substances(including local anesthetics, LAs)in cosmetics, which has been successfully applied in the analysis of actual samples. This work aims to develop a more convenient high performance liquid chromatography triple quadrupole mass spectrometry(HPLC-QQQ-MS/MS)method for the quantitative determination of LAs. Samples were ultrasonically extracted with methanol, separated on an Agilent Poroshell 120 EC-C18 column(2.1 mm × 100 mm, 2.7 μm), and eluted with a gradient mobile phase consisting of 0.1% formic acid aqueous solution and methanol. Quantification was performed using the external standard method. The results show that all 23 LAs are effectively separated within 12 minutes, with good linearity in the corresponding concentration ranges and the correlation coefficients all greater than 0.99. The limits of detection(LOD)range from 0.002 5 to 0.05 μg/g, and the limits of quantification(LOQ)range from 0.01 to 0.1 μg/g. The average recoveries of the 23 LAs in 5 blank cosmetic matrices are 80.68%-117.57%, with the relative standard deviations(RSDs)less than 5.98%. This method has good precision and high accuracy, and is suitable for the determination of LAs in 5 cosmetic matrices.

Key words: local anesthetics, chemical analysis, ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry(UPLC-Q-TOF-MS), high performance liquid chromatography triple quadrupole mass spectrometry(HPLC-QQQ-MS/MS)

中图分类号: 

  • TQ658